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Journal Articles

Rltpr Is a Central Scaffold Protein Regulating Human TCR Co-Signaling and Cytoskeletal Dynamics

Tilmann Schober, MD, Thomas Magg, PhD, Melanie Laschinger, PhD, Thomas Fröhlich, PhD, Meino Rohlfs, PhD, Yanshan Liu, PhD, Jacek Puchalka, PhD, Tanja Weisser, Karin Fehlner, PhD, Christoph Walz, MD, Natália Duarte Linhares, PhD, Sérgio D. Pena, MD PhD, Bernd H. Belohradsky, MD, Christoph Klein, MD PhD, Fabian Hauck, MD PhD

Blood (2016) 128 (22): 131.

https://doi.org/10.1182/blood.V128.22.131.131

Published: 2016

Journal Articles

SWI/SNF Protein SMARCD2 Orchestrates Transcriptional Networks Controlling Hematopoiesis and Neutrophil Granulocytes in Humans, Mice and Zebrafish

Blood (2016) 128 (22): 2.

https://doi.org/10.1182/blood.V128.22.2.2

Published: 2016

Journal Articles

A Human Bone Marrow Failure Syndrome Caused By a Homozygous Mutation in MYSM1

Ehsan Bahrami, Tomas Racek, PhD, Maximilian Witzel, MD, Jacek Puchalka, PhD, Naschla Greif-Kohistani, MD, Daniel Kotlarz, MD PhD, Michael Orth, PhD, Kirsten Lauber, PhD, Christoph Walz, MD, Waleed Al Herz, MD, Hans-Peter Horny, MD, Heinrich Schmidt, MD, Michael H. Albert, MD, Christoph Klein, MD PhD

Blood (2015) 126 (23): 1204.

https://doi.org/10.1182/blood.V126.23.1204.1204

Published: 2015

Journal Articles

Regulation of Transcription Factors Foxp1, E2A and Egr-1 By microRNA-191 Constrains B Lymphocyte Development and Suppresses Development of Diffuse Large B Cell Lymphoma

Marcin Lyszkiewicz, PhD, Jonas Blume, PhD, Natalia Zietara, PhD, Katrin Witzlau, Jacek Puchalka, PhD, Namita Saran, PhD, Sandra Duber, PhD, Roy Bishnudeo, PhD, Siegfried Weiss, PhD, Andreas Krueger, PhD Prof.

Blood (2015) 126 (23): 287.

https://doi.org/10.1182/blood.V126.23.287.287

Published: 2015

Journal Articles

Limited niche availability suppresses murine intrathymic dendritic-cell development from noncommitted progenitors

Marcin Łyszkiewicz, Natalia Ziętara, Lisa Föhse, Jacek Puchałka, Jana Diestelhorst, Katrin Witzlau, Immo Prinz, Axel Schambach, Andreas Krueger

Blood (2015) 125 (3): 457–464.

https://doi.org/10.1182/blood-2014-07-592667

Published: 2015

Includes: Supplemental data

Journal Articles

A Rare Case of Congenital Atransferrinemia: International Collaboration for Genetic Diagnosis

Hanan Nazir, MD, Murtadha K. Al-Khabori, MD MSc, FRCPC, Naschla Kohistani, MD, Jacek Puchalka, PhD, Christoph Klein, MD PhD

Blood (2014) 124 (21): 4883.

https://doi.org/10.1182/blood.V124.21.4883.4883

Published: 2014

Journal Articles

Inherited biallelic CSF3R mutations in severe congenital neutropenia

Blood (2014) 123 (24): 3811–3817.

https://doi.org/10.1182/blood-2013-11-535419

Published: 2014

Includes: Supplemental data

Journal Articles

Inherited Biallelic Loss-Of-Function Mutations In CSF3R Define a Novel Type Of Severe Congenital Neutropenia With Full Myeloid Cell Maturation and Refractoriness To RhG-CSF

Alexa Triot, Päivi M Järvinen, Juan I. Arostegui, MD, Tomas Racek, PhD, Jacek Puchalka, Jose Luis Dapena Díaz, MD, Naschla Kohistani, MD, E. Michael Gertz, PhD, Alejandro A. Schäffer, Cristina Díaz de Heredia Rubio, MD, Mehmet A. Ozdemir, MD, Turkan Patiroglu, MD, Musa Karakukcu, MD, José Sanchez de Toledo Codina, MD, Jordi Yagüe, MD, PhD, Ekrem Unal, Christoph Klein, MD PhD

Blood (2013) 122 (21): 1025.

https://doi.org/10.1182/blood.V122.21.1025.1025

Published: 2013

Journal Articles

Novel NGS-Based Platforms For Molecular Diagnosis Of Severe Congenital Neutropenia

Tomas Racek, PhD, Jacek Puchalka, PhD, Naschla Kohistani, MD, Christoph Klein, MD PhD

Blood (2013) 122 (21): 1034.

https://doi.org/10.1182/blood.V122.21.1034.1034

Published: 2013

Journal Articles

Deficiency Of JAGN1 Causes Severe Congenital Neutropenia Associated With Defective Secretory Pathway and Aberrant Myeloid Cell Homeostasis

Blood (2013) 122 (21): 439.

https://doi.org/10.1182/blood.V122.21.439.439

Published: 2013

Journal Articles

G6PC3 Deficiency Associated with Congenital Neutropenia and Enterocolitis

Jana Diestelhorst, Daniel Kotlarz, Giridharan Appaswamy, PhD, Rita Beier, MD, Peter M Krawitz, MD, PhD, Peter N Robinson, MD, PhD, Jochen Hecht, PhD, Jacek Puchalka, PhD, Alejandro A. Schäffer, PhD, Dietmar Pfeifer, PhD, Ulrich Baumann, MD, Eva-Doreen Pfister, MD, Gudrun Brandes, PhD, Gabriella Palla, MD, Roland Jacobs, PhD, Hans H. Kreipe, MD, Stefan Mundlos, MD, Christoph Klein, MD, PhD

Blood (2011) 118 (21): 2170.

https://doi.org/10.1182/blood.V118.21.2170.2170

Published: 2011

NARROW

Rltpr Is a Central Scaffold Protein Regulating Human TCR Co-Signaling and Cytoskeletal Dynamics

SWI/SNF Protein SMARCD2 Orchestrates Transcriptional Networks Controlling Hematopoiesis and Neutrophil Granulocytes in Humans, Mice and Zebrafish

A Human Bone Marrow Failure Syndrome Caused By a Homozygous Mutation in MYSM1

Regulation of Transcription Factors Foxp1, E2A and Egr-1 By microRNA-191 Constrains B Lymphocyte Development and Suppresses Development of Diffuse Large B Cell Lymphoma

Limited niche availability suppresses murine intrathymic dendritic-cell development from noncommitted progenitors

A Rare Case of Congenital Atransferrinemia: International Collaboration for Genetic Diagnosis

Inherited biallelic CSF3R mutations in severe congenital neutropenia

Inherited Biallelic Loss-Of-Function Mutations In CSF3R Define a Novel Type Of Severe Congenital Neutropenia With Full Myeloid Cell Maturation and Refractoriness To RhG-CSF

Novel NGS-Based Platforms For Molecular Diagnosis Of Severe Congenital Neutropenia

Deficiency Of JAGN1 Causes Severe Congenital Neutropenia Associated With Defective Secretory Pathway and Aberrant Myeloid Cell Homeostasis

G6PC3 Deficiency Associated with Congenital Neutropenia and Enterocolitis

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American Society of Hematology

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American Society of Hematology

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